Disease Directory Young-onset Parkinson disease
Neurological

Young-onset Parkinson disease

Type

Disease

Gene

SYNJ1, SNCA, PINK1, UCHL1, HTRA2, PODXL

About Young-onset Parkinson disease

Young-onset Parkinson disease is a rare disease catalogued by Orphanet (ORPHA:2828). It is associated with the SYNJ1, SNCA, PINK1 genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Young-onset Parkinson disease trials.

Search ClinicalTrials.gov for "Young-onset Parkinson disease" or filter by Orphanet code ORPHA:2828 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:2828)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Young-onset Parkinson disease trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Young-onset Parkinson disease. Updated daily.